ClinVar Miner

Submissions for variant NM_015973.5(GAL):c.*15T>C

gnomAD frequency: 0.61580  dbSNP: rs1042577
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001703312 SCV001933712 benign Familial temporal lobe epilepsy 8 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718955 SCV005319270 benign not provided criteria provided, single submitter not provided

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